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Blood Pressure Management Pre- and Post-Reperfusion in Acute Ischemic Stroke: Evidence and Insights from Recent Studies. 急性缺血性卒中再灌注前后的血压管理:最新研究的证据和见解。
IF 5.2 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-25 DOI: 10.1007/s11910-025-01443-5
Feifeng Liu, Craig S Anderson

Purpose of review: Effective control of blood pressure (BP) is potentially a critical determinant in making a successful recovery from acute ischemic stroke. BP is often elevated after the onset of this critical illness, and it is related to both the severity of the ischemic injury and subsequent changes in cerebral perfusion and collateral blood flow. However, recent studies have challenged longstanding assumptions over the safety and efficacy of BP lowering in being able to reduce the risk of reperfusion injury in acute ischemic stroke. This review synthesizes contemporary evidence and discusses the evolving landscape of BP management in acute ischemic stroke.

Recent findings: Three prehospital ambulance-initiated trials of early BP lowering in patients with undifferentiated stroke have shown neutral or adverse effects, while the results of multiple trials of in-hospital management BP lowering in patients who have received successful reperfusion therapy for acute ischemic stroke due to large-vessel occlusion highlight the risks of over-aggressive treatment. Despite considerable research effort, the optimal BP management strategy in acute ischemic stroke remains uncertain, although avoiding excessive reductions appears critical.

综述的目的:有效控制血压(BP)可能是急性缺血性卒中成功康复的关键决定因素。这种危重疾病发病后血压常升高,它与缺血性损伤的严重程度以及随后脑灌注和侧支血流量的变化有关。然而,最近的研究挑战了长期以来关于降低血压能够降低急性缺血性卒中再灌注损伤风险的安全性和有效性的假设。这篇综述综合了当代的证据,并讨论了急性缺血性卒中中血压管理的发展前景。最近的研究发现:三项院前救护车启动的对未分化脑卒中患者早期降压的试验显示出中性或不良影响,而对因大血管闭塞而急性缺血性脑卒中患者成功接受再灌注治疗的住院管理降压的多项试验结果强调了过度积极治疗的风险。尽管进行了大量的研究,但急性缺血性卒中的最佳血压管理策略仍然不确定,尽管避免过度降低似乎至关重要。
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引用次数: 0
Selective Visual Attention in ADHD: A Narrative Review. ADHD的选择性视觉注意:一个叙述性的回顾。
IF 5.2 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-24 DOI: 10.1007/s11910-025-01435-5
Jennifer L Klein, Harriet A Allen, John Clibbens, Amy Cook, Virginia Amanatidou, Eirini Mavritsaki

Purpose of review: Attention-deficit/hyperactivity disorder is a common neurodevelopmental disorder characterized by impairing levels of inattention, hyperactivity and impulsivity that adversely impact functioning across social, academic/occupational and home settings. While the name of the disorder implies obvious difficulties in attention, research has struggled to consistently identify a precise neurocognitive marker. This article aims to characterize the functioning of selective visual attention in ADHD by reviewing previous studies that compare individuals with ADHD and healthy controls at the behavioral and neural levels using single-frame visual search tasks.

Recent findings: Past research indicates both bottom-up (stimulus-driven) and top-down (goal-driven) attention across both time and space are likely affected in ADHD. However, more research is needed to illuminate the specific mechanisms involved. Ultimately, this narrative review aims to highlight the importance of studying selective visual attention in ADHD to explain the heterogeneous symptoms and impairments of this complex disorder, as well as to build a stronger bridge between the high-level behaviors of ADHD and their underlying neurobiological mechanisms.

回顾目的:注意缺陷/多动障碍是一种常见的神经发育障碍,其特征是注意力不集中、多动和冲动的程度受损,对社会、学业/职业和家庭环境的功能产生不利影响。虽然这种疾病的名字暗示了明显的注意力障碍,但研究一直在努力确定一种精确的神经认知标记。本文旨在通过回顾以往的研究,在单帧视觉搜索任务中比较ADHD患者和健康对照者在行为和神经水平上的选择性视觉注意的功能。最近的发现:过去的研究表明,自下而上(刺激驱动)和自上而下(目标驱动)的注意力在时间和空间上都可能受到ADHD的影响。然而,需要更多的研究来阐明所涉及的具体机制。最后,这篇叙述性综述旨在强调研究ADHD中选择性视觉注意的重要性,以解释这种复杂疾病的异质性症状和损伤,并在ADHD的高级行为与其潜在的神经生物学机制之间建立更强的桥梁。
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引用次数: 0
Pregnancy Outcomes in Epilepsy Patients Treated with Neuromodulating Devices. 神经调节装置治疗癫痫患者妊娠结局
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-21 DOI: 10.1007/s11910-025-01441-7
Lu Lin, Yi Li

Purpose of review: Neuromodulation provides additional treatment options for patients with drug-resistant epilepsy who are not candidates or unwilling to undergo resective or ablative surgery. However, our current knowledge on the safety and efficacy of different neuromodulating devices during pregnancy is limited. This article reviews recent research on pregnancy outcomes in epilepsy patients treated with vagus nerve stimulation (VNS), deep brain stimulation (DBS), or responsive neurostimulation (RNS).

Recent findings: Currently available information about pregnancy outcomes in epilepsy patients with neuromodulating devices all comes from cases series or case reports. Randomized control trials or prospective observational studies are lacking in this patient population. The overall sample size is too small to draw conclusions on the safety of these neuromodulating devices in pregnancy and maternal outcomes including obstetric complications. There is no clear sign of device-related teratogenicity. Further research should be directed at establishing a pregnancy registry and conducting multi-center prospective studies to track pregnancy outcomes in epilepsy patients with various neuromodulating devices.

综述目的:神经调节为不适合或不愿接受切除或消融手术的耐药癫痫患者提供了额外的治疗选择。然而,我们目前对怀孕期间不同神经调节装置的安全性和有效性的了解是有限的。本文综述了迷走神经刺激(VNS)、脑深部刺激(DBS)和反应性神经刺激(RNS)治疗癫痫患者妊娠结局的最新研究进展。最新发现:目前可获得的关于使用神经调节装置的癫痫患者妊娠结局的信息均来自病例系列或病例报告。该患者群体缺乏随机对照试验或前瞻性观察性研究。总体样本量太小,无法得出这些神经调节装置在妊娠和孕产妇结局(包括产科并发症)中的安全性的结论。没有明显的器械相关致畸迹象。进一步的研究应着眼于建立妊娠登记并开展多中心前瞻性研究,以跟踪使用各种神经调节装置的癫痫患者的妊娠结局。
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引用次数: 0
The Gray Zone of Consciousness: Cognitive Motor Dissociation. 意识的灰色地带:认知运动分离。
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-18 DOI: 10.1007/s11910-025-01438-2
Daniel Kondziella

Purpose of review: Covert consciousness, including cognitive motor dissociation (CMD), occurs in clinically unresponsive patients with brain injury who can willfully modulate their brain activity to comply with motor imagery commands as revealed by functional magnetic resonance imaging, EEG or other technologies. In 2024, the Curing Coma Campaign conducted a gap analysis of the field of covert consciousness and CMD. This article discusses the achievements that have been made in the field since then.

Recent findings: Three major recent achievements include epidemiological data that CMD occurs in up to 25% of unresponsive brain injury patients, the development of convenient tools for detecting CMD at the bedside, and CMD as a biomarker of cerebral reserves that may possibly be exploited pharmacologically for prognostication and rehabilitation. Although many questions remain, recent findings have paved the way for the implementation of CMD screening in clinical routine, also in resource-poor settings, for better prognostication after brain injury and possibly for therapeutic purposes.

综述目的:脑损伤临床无反应患者存在隐性意识,包括认知运动分离(CMD),这些患者可以通过功能磁共振成像、脑电图或其他技术显示有意调节其脑活动以服从运动图像命令。2024年,“治愈昏迷运动”对隐蔽意识和CMD领域进行了差距分析。本文讨论了自那时以来在该领域取得的成就。最近的发现:最近的三个主要成就包括流行病学数据表明,高达25%的无反应性脑损伤患者发生CMD,在床边检测CMD的便捷工具的开发,以及CMD作为脑储备的生物标志物,可能在药理学上用于预测和康复。尽管仍存在许多问题,但最近的研究结果为在临床常规中以及在资源贫乏的环境中实施CMD筛查铺平了道路,以便更好地预测脑损伤后的预后,并可能用于治疗目的。
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引用次数: 0
Approach to Eye Pain: Differential Diagnosis and Work Up for the Neurologist. 眼痛的方法:神经科医生的鉴别诊断和工作。
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-12 DOI: 10.1007/s11910-025-01436-4
Jennifer Robblee, Jay N Patel

Purpose of review: Eye pain is a common but diagnostically complex symptom. The underlying etiologies span neurologic, ophthalmologic, and systemic conditions that range from benign to vision- or life-threatening. This review aims to provide a neurologist-oriented approach to the differential diagnosis of eye pain, emphasizing clinical reasoning and red flag identification.

Recent findings: Ocular inflammation and surface disorders are commonly diagnosed etiologies for eye pain but neurologic disorders including primary headaches may be underrecognized sources of eye pain. Clinical clues like the pain description and location, patterns of visual disturbances, and other associated symptoms can guide diagnosis. Exam clues like optic disc edema, cranial nerve abnormalities, red eye pattern, ocular bruit, and intraocular pressure can guide localization and referral urgency. Integration of targeted history, key physical exam findings, and judicious use of investigations are critical for identifying vision- or life-threatening pathology. Using a focused history with targeted neurologic and ophthalmologic examinations, neurologists will be able to choose appropriate investigations and identify when urgent ophthalmology referral is required. This review outlines a systematic, symptom-based approach to eye pain so that neurologists can identify urgent conditions, improve diagnostic efficiency, and collaborate effectively with ophthalmology.

回顾目的:眼痛是一种常见但诊断复杂的症状。潜在的病因包括神经、眼科和全身疾病,从良性到视力或危及生命。这篇综述的目的是提供一个以神经学家为导向的方法来鉴别诊断眼痛,强调临床推理和危险信号识别。最近发现:眼炎症和眼表疾病是眼痛的常见病因,但包括原发性头痛在内的神经系统疾病可能是眼痛的未被充分认识的病因。临床线索,如疼痛的描述和位置,视觉障碍的模式,以及其他相关症状可以指导诊断。视盘水肿、颅神经异常、红眼、眼瘀伤、眼压等检查线索可指导定位和转诊急症。整合目标病史、关键体检结果和明智地使用调查对于识别视力或危及生命的病理至关重要。通过有针对性的神经和眼科检查,神经科医生将能够选择适当的调查,并确定何时需要紧急眼科转诊。这篇综述概述了一种系统的,基于症状的方法来治疗眼痛,以便神经科医生能够识别紧急情况,提高诊断效率,并与眼科有效合作。
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引用次数: 0
Rehabilitation Strategies for Sleep and Autonomic Symptoms in Parkinson's Disease. 帕金森病睡眠和自主神经症状的康复策略。
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-08 DOI: 10.1007/s11910-025-01433-7
Hikaru Kamo, Koichi Nagaki, Lisa Warren, Alison R Kraus, Michael S Okun, Aparna Wagle Shukla

Purpose of review: To evaluate the effectiveness of rehabilitation therapies for managing symptoms of sleep and autonomic dysfunction (cardiovascular, gastrointestinal, urinary and sexual) in Parkinson's disease (PD). The narrative review focuses on recent data drawn from clinical trials, particularly randomized controlled trials, to assess these therapies and the overall quality of the evidence.

Recent findings: Resistance training and aerobic exercises can improve sleep quality in PD. Resistance and aerobic exercises, along with abdominal binders, may help alleviate orthostatic hypotension, though the quality of evidence is not high. Interventions such as expiratory muscle strength training, sensorimotor training, and video-assisted swallowing therapy are beneficial for dysphagia. Pelvic floor muscle training combined with behavioral therapy can potentially mitigate urgency and urge incontinence. Many rehab-based strategies though promising lack sufficient evidence for implementation into clinical practice. The current evidence supports their role in addressing sleep disturbances, orthostatic hypotension and dysphagia. However, the evidence for their effectiveness in treating gastroparesis, constipation, and urinary and sexual dysfunction remains limited.

综述目的:评价康复治疗对帕金森病(PD)患者睡眠和自主神经功能障碍(心血管、胃肠、泌尿和性)症状的治疗效果。叙述性综述侧重于从临床试验,特别是随机对照试验中提取的最新数据,以评估这些疗法和证据的总体质量。最新发现:阻力训练和有氧运动可以改善PD患者的睡眠质量。阻力和有氧运动,以及腹部束缚,可能有助于缓解直立性低血压,尽管证据质量不高。干预措施,如呼气肌力训练,感觉运动训练,视频辅助吞咽治疗是有益的吞咽困难。盆底肌肉训练结合行为疗法可以潜在地减轻急迫性和急迫性尿失禁。许多基于康复的策略虽然有希望,但缺乏足够的证据来实施临床实践。目前的证据支持它们在解决睡眠障碍、体位性低血压和吞咽困难方面的作用。然而,它们在治疗胃轻瘫、便秘、泌尿和性功能障碍方面的有效性证据仍然有限。
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引用次数: 0
Uncommon Non-MS Demyelinating Disorders of the Central Nervous System. 罕见的非ms中枢神经系统脱髓鞘疾病。
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-01 DOI: 10.1007/s11910-025-01432-8
Angshuman Mukherjee, Debasis Roy, Ambar Chakravarty

Purpose of review: Definitive diagnosis of multiple sclerosis (MS) requires exclusion of other central nervous system (CNS) disorders sharing similar clinical, pathological and radiological features. In this review we discuss some relatively uncommon disorders with special emphasis on their differentiation from MS clinically and radiologically. While most conditions have a demyelinating pathology, a few very important mimics may have a non-demyelinating pathology to merit some discussion.

Recent findings: Two major areas of diagnostic advances have been made in recent times, the recognition of neuromyelitis optica spectrum disorder (NMOSD), and the myelin oligodendrocyte antibody mediated disorder (MOGAD). These two entities are mediated by completely different antibodies detectable in peripheral blood samples by enzyme-linked immunosorbent assay (ELISA) or cell-based assays and produce clinical disorders could be differentiated from MS by their clinical features, disease course, prognosis, and imaging features. NMOSD is a rare CNS autoimmune disease that predominantly targets the spinal cord, optic nerves and brainstem. In sixty to eighty% of cases of NMOSD, optic neuritis (ON) and/or longitudinally extensive transverse myelitis (LETM) result in blindness and paralysis. In NMOSD these are associated with a serological antibody to aquaporin-4 (AQP4). AQP4 is a water channel protein found in many organs, but in the CNS, AQP4 is expressed in a perivascular distribution on astrocytic foot processes around blood vessels and the glia limitans (glymphatic). Comparative studies of AQP4-seropositive and AQP4- seronegative NMOSD cohorts note that some of the seronegative NMOSD cases tend to differ from the seropositive cases in several aspects: bilateral optic neuritis, simultaneous optic neuritis and transverse myelitis, younger age at onset, and an apparently monophasic course. This prompted search for putative antibodies other than AQP4. MOG antibody disease is a CNS autoimmune disease associated with a serological antibody against myelin oligodendrocyte glycoprotein (MDG). MOG is a glycoprotein expressed on the outer membrane of myelin and solely found within the CNS, including the brain, optic nerves and spinal cord. Clinically, the disease resembles NMOSD in its predilection for relapses of optic neuritis and transverse myelitis. In addition, acute disseminated encephalomyelitis (ADEM) is a well-recognized phenotype of MOG antibody disease in children. About 42% of NMOSD patients who test seronegative for the AQP4 antibody test positive for MOG antibodies. MOG antibody disease has thus recently emerged as a distinct entity in a sizable portion of the patient population diagnosed with NMOSD or even MS. The second field where significant progress has been made is the recently modified McDonald criteria proposed at the ECTRIMS (European Committee (2024) for Treatment and Research in Multiple Sclerosis) which i

综述目的:多发性硬化症(MS)的明确诊断需要排除其他具有相似临床、病理和影像学特征的中枢神经系统(CNS)疾病。在这篇综述中,我们讨论了一些相对罕见的疾病,特别强调了它们与MS的临床和影像学鉴别。虽然大多数情况有脱髓鞘病理,一些非常重要的模拟可能有非脱髓鞘病理值得讨论。最近的发现:近年来在诊断方面取得了两大进展,即对视神经脊髓炎谱系障碍(NMOSD)和髓鞘少突胶质细胞抗体介导障碍(MOGAD)的识别。这两种实体由完全不同的抗体介导,可通过酶联免疫吸附试验(ELISA)或基于细胞的检测在外周血样本中检测到,并产生临床疾病,可通过其临床特征、病程、预后和影像学特征与MS区分。NMOSD是一种罕见的中枢神经系统自身免疫性疾病,主要以脊髓、视神经和脑干为靶点。在60%到80%的NMOSD病例中,视神经炎(ON)和/或纵向广泛的横脊髓炎(LETM)导致失明和瘫痪。在NMOSD中,这些与水通道蛋白-4 (AQP4)的血清学抗体相关。AQP4是一种存在于许多器官中的水通道蛋白,但在中枢神经系统中,AQP4在血管周围的星形细胞足突和胶质细胞(淋巴细胞)的血管周围分布表达。AQP4-血清阳性和AQP4-血清阴性NMOSD队列的比较研究发现,一些血清阴性NMOSD病例在几个方面与血清阳性病例有所不同:双侧视神经炎,同时视神经炎和横断面脊髓炎,发病年龄更小,病程明显为单相。这促使人们寻找除AQP4以外的推定抗体。MOG抗体病是一种与髓鞘少突胶质细胞糖蛋白(MDG)血清学抗体相关的中枢神经系统自身免疫性疾病。MOG是一种表达于髓鞘外膜的糖蛋白,仅存在于中枢神经系统,包括脑、视神经和脊髓。临床上,该疾病与NMOSD相似,其倾向于视神经炎和横脊髓炎的复发。此外,急性播散性脑脊髓炎(ADEM)是儿童MOG抗体疾病的一种公认的表型。约42% AQP4抗体血清检测阴性的NMOSD患者MOG抗体检测阳性。因此,MOG抗体疾病最近在相当一部分被诊断为NMOSD甚至ms的患者群体中作为一个独特的实体出现。第二个取得重大进展的领域是最近在ECTRIMS(欧洲多发性硬化症治疗和研究委员会(2024))提出的修改的McDonald标准,其中包括三个新特征-中央静脉征象(CVS)和顺磁环病变(PRL)。以及脑脊液kappa自由轻链(kFLC)。CVS指的是MS病变中间的血管,在MRI上可见。PRL是指活跃MS病变边缘的铁环,也可以通过MRI检测到。最后,kFLC是由白细胞产生的分子,现在被认为是相当于脑脊液寡克隆带的诊断性生物标志物。这一新标准完善了MRI诊断多发性硬化症的必要性。非多发性硬化症的中枢神经系统脱髓鞘疾病的清单是巨大的。大多数情况是免疫介导的。本文对NMOSD和MOGAD的诊断和治疗进行了讨论,并对ADEM进行了简要讨论。一些罕见的疾病,如抗磷脂综合征、Behcet病、慢性淋巴细胞炎症伴脑桥血管周围增强类固醇反应(CLIPPERS),以及类似ms的Susac综合征也受到了关注。自体炎症综合征是一组新描述的疾病,越来越多地被认为是可引起全身和神经系统疾病的疾病,本文简要讨论了这些疾病。先天免疫系统异常激活,如对抗自身免疫性疾病时,适应性免疫系统参与其中。非免疫介导的条件也可引起或模拟脱髓鞘。病因包括药物、毒素、感染和肿瘤状况。原发性和继发性中枢神经系统淋巴瘤可能与MS斑块相似。包括细菌、病毒和寄生虫感染在内的感染也可能产生类似ms - COVID - 19相关CNS病变和PML的白质信号异常。基因检测,包括全外显子组测序,已经导致白质营养不良表型谱的扩大,在一些非典型MS病例中,诊断被修改为某种形式的白质营养不良。 已经讨论了可以模拟MS的脑白质营养不良的类型。纵向广泛脊髓病变(LECL)可发生在脱髓鞘(LETM)和其他情况下,并且非常重要的是区分彼此,以便提供适当的管理。最后,常见的血管病变,如脂透明质沉积症引起的腔隙,也可能类似于MS斑块,在这一类中,更广泛的病变,如CADASIL,一种具有特定遗传标记的常染色体显性遗传病,需要分化。
{"title":"Uncommon Non-MS Demyelinating Disorders of the Central Nervous System.","authors":"Angshuman Mukherjee, Debasis Roy, Ambar Chakravarty","doi":"10.1007/s11910-025-01432-8","DOIUrl":"https://doi.org/10.1007/s11910-025-01432-8","url":null,"abstract":"<p><strong>Purpose of review: </strong>Definitive diagnosis of multiple sclerosis (MS) requires exclusion of other central nervous system (CNS) disorders sharing similar clinical, pathological and radiological features. In this review we discuss some relatively uncommon disorders with special emphasis on their differentiation from MS clinically and radiologically. While most conditions have a demyelinating pathology, a few very important mimics may have a non-demyelinating pathology to merit some discussion.</p><p><strong>Recent findings: </strong>Two major areas of diagnostic advances have been made in recent times, the recognition of neuromyelitis optica spectrum disorder (NMOSD), and the myelin oligodendrocyte antibody mediated disorder (MOGAD). These two entities are mediated by completely different antibodies detectable in peripheral blood samples by enzyme-linked immunosorbent assay (ELISA) or cell-based assays and produce clinical disorders could be differentiated from MS by their clinical features, disease course, prognosis, and imaging features. NMOSD is a rare CNS autoimmune disease that predominantly targets the spinal cord, optic nerves and brainstem. In sixty to eighty% of cases of NMOSD, optic neuritis (ON) and/or longitudinally extensive transverse myelitis (LETM) result in blindness and paralysis. In NMOSD these are associated with a serological antibody to aquaporin-4 (AQP4). AQP4 is a water channel protein found in many organs, but in the CNS, AQP4 is expressed in a perivascular distribution on astrocytic foot processes around blood vessels and the glia limitans (glymphatic). Comparative studies of AQP4-seropositive and AQP4- seronegative NMOSD cohorts note that some of the seronegative NMOSD cases tend to differ from the seropositive cases in several aspects: bilateral optic neuritis, simultaneous optic neuritis and transverse myelitis, younger age at onset, and an apparently monophasic course. This prompted search for putative antibodies other than AQP4. MOG antibody disease is a CNS autoimmune disease associated with a serological antibody against myelin oligodendrocyte glycoprotein (MDG). MOG is a glycoprotein expressed on the outer membrane of myelin and solely found within the CNS, including the brain, optic nerves and spinal cord. Clinically, the disease resembles NMOSD in its predilection for relapses of optic neuritis and transverse myelitis. In addition, acute disseminated encephalomyelitis (ADEM) is a well-recognized phenotype of MOG antibody disease in children. About 42% of NMOSD patients who test seronegative for the AQP4 antibody test positive for MOG antibodies. MOG antibody disease has thus recently emerged as a distinct entity in a sizable portion of the patient population diagnosed with NMOSD or even MS. The second field where significant progress has been made is the recently modified McDonald criteria proposed at the ECTRIMS (European Committee (2024) for Treatment and Research in Multiple Sclerosis) which i","PeriodicalId":10831,"journal":{"name":"Current Neurology and Neuroscience Reports","volume":"25 1","pages":"45"},"PeriodicalIF":4.8,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144539362","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cerebrovascular and Peripheral Vascular Complications in Cancer Patients. 肿瘤患者的脑血管和外周血管并发症。
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-07-01 DOI: 10.1007/s11910-025-01434-6
Julien Rousseau, Patrick Y Wen

Purpose of this review: This review explores the complex relationship between cancer and vascular disease. It aims to synthesize current evidence on the epidemiology, mechanisms, management, and outcomes of ischemic stroke, cerebral venous sinus thrombosis (CVST), venous thromboembolism (VTE) in brain tumor patients, and intracranial hemorrhage (ICH), while highlighting the cerebrovascular risks of systemic cancer therapies.

Recent findings: Recent studies reveal that cancer patients are at increased risk for ischemic stroke, often from cancer-specific mechanisms such as hypercoagulability, non-bacterial thrombotic endocarditis, and tumor embolism. VTE is increasingly recognized in patients with primary brain tumors. Emerging data support the safety of direct oral anticoagulants over low-molecular weight heparin in selected patients with brain tumors. Cancer treatments-including immune checkpoint inhibitors (ICIs), hormonal therapies, and radiation-contribute to cerebrovascular risk. Vascular complications are underrecognized yet significant contributors to morbidity and mortality in cancer patients. Multidisciplinary strategies, personalized risk stratification, and targeted research are critical to improving outcomes in this vulnerable population.

本文目的:探讨肿瘤与血管疾病之间的复杂关系。旨在综合缺血性脑卒中、脑静脉窦血栓形成(CVST)、脑肿瘤患者静脉血栓栓塞(VTE)和颅内出血(ICH)的流行病学、机制、管理和结局的现有证据,同时强调系统性癌症治疗的脑血管风险。最近的发现:最近的研究表明,癌症患者发生缺血性卒中的风险增加,通常来自癌症特异性机制,如高凝性、非细菌性血栓性心内膜炎和肿瘤栓塞。静脉血栓栓塞越来越多地出现在原发性脑肿瘤患者中。新出现的数据支持在选定的脑肿瘤患者中直接口服抗凝剂比低分子肝素更安全。癌症治疗——包括免疫检查点抑制剂(ICIs)、激素治疗和放疗——会增加脑血管风险。血管并发症是癌症患者发病率和死亡率的重要因素,但尚未得到充分认识。多学科策略、个性化风险分层和有针对性的研究对于改善这一弱势群体的预后至关重要。
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引用次数: 0
Intracranial Recordings in Epilepsy: an Approach to Understanding the Neural Mechanisms of Social Cognition. 癫痫的颅内记录:一种理解社会认知神经机制的方法。
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-06-28 DOI: 10.1007/s11910-025-01431-9
Kaitlyn E Davis, Rajesh K Kana, Jerzy P Szaflarski

Purpose of review: Social cognition, especially theory of mind (ToM), is often impaired in clinical populations including epilepsy, with serious consequences for quality of life. This review synthesizes evidence from clinical assessments, neuroimaging, and intracranial recording techniques to examine how social cognitive processes are represented in the human brain and how they may be disrupted in epilepsy. Emphasis is placed on the emerging contributions of intracranial electroencephalography (iEEG) and intracranial electrical stimulation (iES) to this field.

Recent findings: While the literature using iEEG/iES to investigate social cognition remains limited, recent studies have begun to map the spatiotemporal and causal underpinnings of ToM and related functions. This work complements behavioral and fMRI findings and suggests avenues for translational research. Intracranial techniques represent a promising tool for advancing social cognitive neuroscience. Integrating this approach with clinical data and established behavioral paradigms can enhance our understanding of social cognition and improve care for populations with focal epilepsy.

综述目的:社会认知,特别是心理理论(ToM),在包括癫痫在内的临床人群中经常受损,对生活质量造成严重后果。本综述综合了来自临床评估、神经影像学和颅内记录技术的证据,以研究社会认知过程如何在人脑中表现,以及它们如何在癫痫中被破坏。重点放在颅内脑电图(iEEG)和颅内电刺激(iES)在这一领域的新兴贡献。最近的发现:虽然使用iEEG/iES研究社会认知的文献仍然有限,但最近的研究已经开始绘制ToM及其相关功能的时空和因果基础。这项工作补充了行为和功能磁共振成像的发现,并为转化研究提供了途径。颅内技术代表了一个有前途的工具,以推进社会认知神经科学。将这种方法与临床数据和已建立的行为范式相结合,可以增强我们对社会认知的理解,并改善对局灶性癫痫人群的护理。
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引用次数: 0
Update on paraproteinemic neuropathy. 副蛋白血症性神经病变的最新进展。
IF 4.8 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-06-23 DOI: 10.1007/s11910-025-01430-w
Rebecca Traub, Samuel M Rubinstein, Christopher Dittus

Purpose of review: This article reviews recent clinical updates and research on the evaluation and management of patients with peripheral neuropathy in association with monoclonal gammopathies.

Recent findings: Recent studies have elucidated pathogenic mechanisms of IgM paraprotein associated neuropathies, including nodal and paranodal targets and complement mediated processes, suggesting novel therapeutic targets. New chemotherapeutic regimens have improved outcomes and neurotoxic side effect profiles in the treatment of patients with light chain (AL) amyloidosis and POEMS syndrome. Establishing when a monoclonal gammopathy is causative of a peripheral neuropathy remains a clinical challenge. New therapeutic drugs for treatment of IgM paraprotein associated neuropathies show promise. Identifying AL amyloidosis and POEMS early in patients presenting with neuropathy are important. Clinical phenotyping and antibody testing are critical to evaluating patients with paraproteins and peripheral neuropathy.

综述目的:本文综述了单克隆伽玛病合并周围神经病变的临床进展和评估与治疗研究。最新发现:最近的研究已经阐明了IgM副蛋白相关神经病的致病机制,包括淋巴结和副淋巴结靶点以及补体介导的过程,提出了新的治疗靶点。新的化疗方案改善了治疗轻链(AL)淀粉样变性和POEMS综合征患者的预后和神经毒性副作用。确定单克隆伽玛病何时引起周围神经病变仍然是一个临床挑战。治疗IgM副蛋白相关神经病的新治疗药物显示出希望。在出现神经病变的患者早期识别AL淀粉样变和POEMS是很重要的。临床表型和抗体检测是评估副蛋白和周围神经病变患者的关键。
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